Quantitative phosphoproteomics reveals molecular pathway network in wheat resistance to stripe rust.

Pengfei Gan, Chunlei Tang, Yi Lu, Chenrong Ren, Hojjatollah Rabbani Nasab, Xufeng Kun, Xiaodong Wang, Liangzhuang Li, Zhensheng Kang, Xiaojie Wang, Jianfeng Wang
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Abstract

Protein phosphorylation plays an important role in immune signaling transduction in plant resistance to pathogens. Wheat stripe rust, caused by Puccinia striiformis f. sp. tritici (Pst), severely devastates wheat production. Nonetheless, the molecular mechanism of wheat resistance to stripe rust remains limited. In this study, quantitative phosphoproteomics was employed to investigate the protein phosphorylation changes in wheat challenged by Pst. A total of 1537 and 2470 differentially accumulated phosphoproteins (DAPs) were identified from four early infection stage (6, 12, 18 and 24 h post-inoculation) in incompatible and compatible wheat-Pst interactions respectively. KEGG analysis revealed that Oxidative Phosphorylation, Phosphatidylinositol Signaling, and MAPK signaling processes are distinctively enriched in incompatible interaction, while Biosynthesis of secondary metabolites and RNA degradation process were significantly enriched in compatible interactions. In particular, abundant changes in phosphorylation levels of chloroplast proteins were identified, suggesting the regulatory role of photosynthesis in wheat-Pst interaction, which is further emphasized by protein-protein interaction (PPI) network analysis. Motif-x analysis identified [xxxxSPxxxx] motif, likely phosphorylation sites for defensive response-related kinases, and a new [xxxxSSxxxx] motif significantly enriched in incompatible interaction. The results shed light on the early phosphorylation events contributing to wheat resistance against Pst. Moreover, our study demonstrated that the phosphorylation levels of Nucleoside diphosphate kinase TaNAPK1 are upregulated at 12 hpi with CYR23 and at 24 hpi with CYR31. Transient silencing of TaNAPK1 was able to attenuate wheat resistance to CYR23 and CYR31. Our study provides new insights into the mechanisms underlying Pst-wheat interactions and may provide database to find potential targets for the development of new resistant varieties.

定量磷酸蛋白组学揭示小麦抗条锈病的分子通路网络
蛋白质磷酸化在植物抵抗病原体的免疫信号转导中发挥着重要作用。由 Puccinia striiformis f. sp. tritici(Pst)引起的小麦条锈病严重破坏了小麦生产。然而,小麦抗条锈病的分子机制仍然有限。本研究采用定量磷酸化蛋白质组学研究了小麦受条锈病侵染后蛋白质磷酸化的变化。在不相容和相容小麦与 Pst 相互作用的四个早期感染阶段(接种后 6、12、18 和 24 h),分别鉴定了 1537 和 2470 个不同累积的磷酸化蛋白(DAPs)。KEGG 分析显示,氧化磷酸化、磷脂酰肌醇信号转导和 MAPK 信号转导过程在不相容相互作用中明显富集,而次生代谢物的生物合成和 RNA 降解过程在相容相互作用中显著富集。特别是叶绿体蛋白磷酸化水平的大量变化,表明光合作用在小麦-Pst 相互作用中的调控作用,蛋白质-蛋白质相互作用(PPI)网络分析进一步强调了这一点。Motif-x分析发现了[xxxxSPxxxxxx]基序,可能是防御反应相关激酶的磷酸化位点,以及在不相容相互作用中显著富集的新[xxxxSSxxxxxx]基序。这些结果揭示了导致小麦抗 Pst 的早期磷酸化事件。此外,我们的研究表明,核苷二磷酸激酶 TaNAPK1 的磷酸化水平在 CYR23 作用 12 hpi 和 CYR31 作用 24 hpi 时上调。瞬时沉默 TaNAPK1 能够减轻小麦对 CYR23 和 CYR31 的抗性。我们的研究为了解 Pst 与小麦相互作用的机制提供了新的视角,并可能为开发新的抗性品种寻找潜在靶标提供数据库。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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